Canonical Allele Identifier: CA345439492

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241672076C>G (hg19) ; chr1:g.241508776C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508776C>G , CM000663.2:g.241508776C>G	GRCh38
NC_000001.10:g.241672076C>G , CM000663.1:g.241672076C>G	GRCh37
NC_000001.9:g.239738699C>G	NCBI36
NG_012338.1:g.15979G>C , LRG_504:g.15979G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1068G>C
ENST00000682162.1:c.594G>C	ENSP00000508203.1:n.594G>C
ENST00000682567.1:n.642G>C
ENST00000683521.1:c.565G>C	ENSP00000506864.1:p.Asp189His
ENST00000684161.1:n.1780G>C
ENST00000684483.1:c.556-16G>C	ENSP00000507894.1:n.556-16G>C
ENST00000366560.4:c.565G>C MANE Select	ENSP00000355518.4:p.Asp189His
ENST00000366560.3:c.565G>C	ENSP00000355518.3:p.Asp189His
NM_000143.3:c.565G>C , LRG_504t1:c.565G>C	NP_000134.2:p.Asp189His
XM_011544132.1:c.337G>C	XP_011542434.1:p.Asp113His
XM_011544132.2:c.337G>C	XP_011542434.1:p.Asp113His
NM_000143.4:c.565G>C MANE Select	NP_000134.2:p.Asp189His